期刊
JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 605, 期 -, 页码 766-778出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.07.130
关键词
Yolk-shell structure; Multi-active component; Peroxymonosulfate; Peroxymonosulfate Catalytic mechanism; Degradation pathways
资金
- National Natural Science Founda-tion of China [21707043, 51908242]
- Independent Culti-vation Program of Innovation Team of Ji'nan City [2019GXRC011]
- Natural Science Foundation of Shandong Province [ZR2017BEE005]
The study focused on the reasonable design of catalyst structure and composition to improve the catalytic performance of advanced oxidation processes (AOPs). By synthesizing hierarchical Co3O4-C@CoSiOx yolk-shell nanoreactors with multiple active components derived from metal-organic frameworks (MOFs), the researchers achieved significant enhancement in catalytic performance for the degradation of ciprofloxacin (CIP). Under optimized conditions, -98.2% of CIP was degraded within 17 minutes, demonstrating low cobalt leaching and excellent reusability of the catalyst.
The reasonable design of the structure and composition of catalysts was essential to improve the catalytic performance of advanced oxidation processes (AOPs). Herein, we reported a simple strategy to synthesize hierarchical Co3O4-C@CoSiOx yolk-shell nanoreactors with multiple active components by using metal-organic frameworks (MOFs). The novel nanoreactors are further used to activate peroxymonosulfate (PMS) for ciprofloxacin (CIP) degradation. The effects of reaction parameters (pH value, co-existing ions, reaction temperature, etc.) on CIP degradation were systematically investigated. Especially, -98.2% of CIP was degraded within 17 min under the optimal conditions, together with the low cobalt leaching and excellent reusability. The appreciable catalytic performance improvement might be due to the synergistic effect of the structure and component design: (1) the hierarchical yolk-shell structure endowed the catalyst with high surface area (similar to 232.47 m(2)/g) and fully exposed active sites; (2) abundant highly active equivalent to Co-OH+ were formed on the surface of CoSiOx; (3) the presence of oxygen vacancies and nitrogen doped carbon promoted the decomposition of PMS through a non-radical process. The results revealed both the radical (SO4 center dot-, center dot OH and O-2(center dot-)) and non-radical (O-1(2) and direct charge transfer) should be responsible for the CIP degradation. Moreover, the possible degradation pathways of CIP were proposed through the identification of intermediates using LC-MS/MS techniques and density functional theory (DFT) calculation. Our work highlights that multi-component catalysts derived from MOFs with novel structure have broad application prospects in AOPs. (C) 2021 Elsevier Inc. All rights reserved.
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